A kit for liver cancer detection
A kit and technology for liver cancer, applied in the field of medical testing, can solve the problems of inability to effectively determine the degree of cancer invasiveness, the significance of diagnosis is not large, and the detection rate of missed diagnosis is high, so as to achieve rapid, sensitive and effective screening judgment and save detection. Cost, simple effect of specimen
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Embodiment 1
[0046] The structure of the kit is as follows: it is equipped with a box body, an ELISA plate located in the box body and a reagent bottle; specifications: 48T / 96T, boxed liquid. The kit includes two parts A1-6 and B1-5:
[0047] 1. A1-6 Reagent part structure and content:
[0048] 1) Buffer solution (PBS): 8g sodium chloride, 0.2g potassium chloride, 2.7g disodium hydrogen phosphate, 0.2g potassium dihydrogen phosphate, add distilled water to 1000ml, pH: 7.0-7.4.
[0049] Dilution of 20× buffer: distilled water is diluted 1:20, that is, 1 part of 20× buffer plus 19 parts of distilled water.
[0050] 2) HRP-labeled LPA antibody: (imported finished product).
[0051] 3) Lysophosphatidic acid (lysophosphatidic acid, LPA) standard substance and negative control substance. (Standard products are imported finished products)
[0052] 4) Washing solution (PBST): PBS solution containing 0.05% Tween-20 (500 μl Tween-20 was added to 1 LPBS and mixed well).
[0053] 5) TMB chromogen...
Embodiment 2
[0064] 1. Part A1-6 testing:
[0065] 1. Take out the required slats from the bag after equilibrating at room temperature for 20 minutes.
[0066] 2. Mark the standard wells, sample wells and blank wells, and add 50 μL of standard substances of different concentrations to each standard well;
[0067] 3. Add 50 μL of the sample to be tested into the sample well; do not add to the blank well.
[0068] 4. Add 100 μL of horseradish peroxidase (HRP)-labeled detection antibody to each well of standard wells and sample wells, seal the reaction wells with plate sealing film, and incubate for 60 min in a 37°C water bath or incubator.
[0069] 5. Discard the liquid, pat dry on absorbent paper, fill each well with washing solution (350 μL), let it stand for 1 min, shake off the washing solution, pat dry on absorbent paper, and repeat washing the plate 5 times (or wash the plate with a plate washer) .
[0070] 6. Add 50 μL each of substrate A and B to each well, and incubate at 37°C in...
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